ES429754A1 - Monoazo and disazo compounds having optionally further substituted 2-acyl-, carboxy- or cyano-benzothienyl diazo component radicals - Google Patents
Monoazo and disazo compounds having optionally further substituted 2-acyl-, carboxy- or cyano-benzothienyl diazo component radicalsInfo
- Publication number
- ES429754A1 ES429754A1 ES429754A ES429754A ES429754A1 ES 429754 A1 ES429754 A1 ES 429754A1 ES 429754 A ES429754 A ES 429754A ES 429754 A ES429754 A ES 429754A ES 429754 A1 ES429754 A1 ES 429754A1
- Authority
- ES
- Spain
- Prior art keywords
- cyano
- signifies
- substituted
- monoazo
- benzothienyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 title 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 title 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 239000000986 disperse dye Substances 0.000 abstract 2
- -1 phenylaminocarbonyl Chemical group 0.000 abstract 2
- 239000000049 pigment Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 238000002425 crystallisation Methods 0.000 abstract 1
- 230000008025 crystallization Effects 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 1
- 239000000835 fiber Substances 0.000 abstract 1
- 230000016615 flocculation Effects 0.000 abstract 1
- 238000005189 flocculation Methods 0.000 abstract 1
- 239000003546 flue gas Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000000976 ink Substances 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- 230000005012 migration Effects 0.000 abstract 1
- 238000013508 migration Methods 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000003973 paint Substances 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000006678 phenoxycarbonyl group Chemical group 0.000 abstract 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N phenyl acetate Chemical compound CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000004033 plastic Substances 0.000 abstract 1
- 229920003023 plastic Polymers 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- 239000002966 varnish Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/32—Preparation of azo dyes from other azo compounds by reacting carboxylic or sulfonic groups, or derivatives thereof, with amines; by reacting keto-groups with amines
- C09B43/38—Preparation of azo dyes from other azo compounds by reacting carboxylic or sulfonic groups, or derivatives thereof, with amines; by reacting keto-groups with amines by reacting two or more ortho-hydroxy naphthoic acid dyes with polyamines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0025—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds
- C09B29/0059—Monoazo dyes prepared by diazotising and coupling from diazotized amino heterocyclic compounds the heterocyclic ring containing only sulfur as heteroatom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Plural Heterocyclic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Compounds free of sulfo groups having the formula < IMAGE > IN WHICH N IS 0, 1 OR 2, R1 signifies halogen, substituted or unsubstituted alkyl, cycloalkyl, alkoxy or cycloalkoxy, trifluoromethyl or nitro, the R1's being the same or different when n is 2, R2 signifies carboxyl, aminocarbonyl, alkylaminocarbonyl, cycloalkylaminocarbonyl, dialkylaminocarbonyl, phenylaminocarbonyl, alkoxycarbonyl, cycloalkoxycarbonyl, phenoxycarbonyl, or cyano, any alkyl, alkoxy, cycloalkyl, cycloalkoxy, phenyl or phenoxy moiety being unsubstituted or substituted, K signifies a coupling component radical, and m is 1 or 2, ARE USEFUL AS PIGMENTS FOR PAINTS, INKS, VARNISHES, PLASTICS, PRINTING PASTES AND PAPER AND DISPERSE DYES FOR SYNTHETIC AND SEMISYNTHETIC FIBERS SUCH AS LINEAR AROMATIC POLYESTERS, CELLULOSE ACETATES AND SYNTHETIC POLYAMIDES. The pigments exhibit notable fastness to, for example, heat, light, weathering, migration, varnishing, solvents, sulfur dioxide and alkalis and resistance to flocculation and crystallization while the disperse dyes possess notable fastness to, for example, light, heat treatments, wet treatments, solvents, lubricants, rubbing, crossdyeing, ozone, flue gases and chlorine.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1281473A CH584257A5 (en) | 1973-09-06 | 1973-09-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES429754A1 true ES429754A1 (en) | 1977-03-01 |
Family
ID=4386615
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES429754A Expired ES429754A1 (en) | 1973-09-06 | 1974-09-04 | Monoazo and disazo compounds having optionally further substituted 2-acyl-, carboxy- or cyano-benzothienyl diazo component radicals |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4055556A (en) |
| JP (1) | JPS5051528A (en) |
| AR (1) | AR206123A1 (en) |
| AU (1) | AU7298274A (en) |
| BE (1) | BE819599A (en) |
| BR (1) | BR7407454D0 (en) |
| CH (1) | CH584257A5 (en) |
| DE (1) | DE2441524A1 (en) |
| ES (1) | ES429754A1 (en) |
| FR (1) | FR2243194B1 (en) |
| GB (1) | GB1471999A (en) |
| IT (1) | IT1019202B (en) |
| NL (1) | NL7411613A (en) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2758818A1 (en) * | 1977-12-30 | 1979-07-12 | Hoechst Ag | NEW CRYSTAL MODIFICATION OF 5- (2'-HYDROXY-3'-NAPHTHOYL-AMINO) -BENZIMIDAZOLONE- (2), METHOD FOR MANUFACTURING AND USING IT |
| JPS5632549A (en) * | 1979-08-27 | 1981-04-02 | Toyo Ink Mfg Co Ltd | Pigment composition |
| JPS56118462A (en) * | 1980-02-25 | 1981-09-17 | Toyo Ink Mfg Co Ltd | Pigment composition |
| US4400318A (en) * | 1980-05-19 | 1983-08-23 | Eastman Kodak Company | Substituted 5-acyl-3-carbamoyl-2-thienyl azo dyes with aniline, tetrahydroquinoline, and benzomorpholine couplers, process of manufacture, and polyamide testile materials dyed therewith |
| DE3344295A1 (en) * | 1983-12-07 | 1985-06-20 | Agfa-Gevaert Ag, 5090 Leverkusen | COLOR PHOTOGRAPHIC RECORDING MATERIAL WITH A COLOR RELEASE FOR BLUE-GREEN DYES, A COLOR IMAGE PRODUCED WITH THESE DYES AND THE DYES ITSELF |
| US4579939A (en) * | 1984-03-16 | 1986-04-01 | Eastman Kodak Company | Azo dyes from substituted 2-aminothiophenes and acyclic active methylene couplers |
| DE3637223A1 (en) * | 1986-11-03 | 1988-05-05 | Bayer Ag | METHOD FOR PRODUCING THIOPHENE COMPOUNDS |
| DE3738374A1 (en) * | 1987-11-12 | 1989-05-24 | Basf Ag | THIEN-3-YLAZO DYES AND THEIR USE |
| DE4420922A1 (en) * | 1994-06-16 | 1995-12-21 | Bayer Ag | Process for the preparation of benzothiophene derivatives |
| BR9713145A (en) | 1996-11-27 | 2000-02-08 | Eastman Chem Co | Process, light-absorbing composition and diacid compounds. |
| EP1369105B1 (en) * | 2002-05-28 | 2008-03-19 | Kao Corporation | Use and method for dyeing hair |
| EP1366752A1 (en) * | 2002-05-28 | 2003-12-03 | Kao Corporation | Hair dye composition |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2338728A (en) * | 1941-09-27 | 1944-01-11 | Eastman Kodak Co | Azo compounds and material colored therewith |
| US2560502A (en) * | 1948-10-22 | 1951-07-10 | Gen Aniline & Film Corp | Metalliferous monoazo dyestuffs |
| US2827450A (en) * | 1955-08-12 | 1958-03-18 | Eastman Kodak Co | 2-aminothiophene azo compounds |
| US2825726A (en) * | 1955-08-12 | 1958-03-04 | Eastman Kodak Co | Monoazo compounds containing a 2-aminothiophene nucleus |
| US2893986A (en) * | 1957-03-08 | 1959-07-07 | American Cyanamid Co | Azo dyes containing the benzonaphthofuranol nucleus |
| GB1123388A (en) * | 1965-12-03 | 1968-08-14 | Acna | Thiophendioxide dyestuffs |
| FR1511695A (en) * | 1966-01-14 | 1968-02-02 | Acna | Dyes for polyamide fibers containing a thiophene dioxide core |
| CH478205A (en) * | 1966-05-23 | 1969-09-15 | Bayer Ag | Process for the preparation of sulfonic acid group-free azo dyes |
| US3849394A (en) * | 1968-01-03 | 1974-11-19 | Ciba Geigy Ag | Monoazo pigments containing a hydroxynaphthoylaminoacridone radical |
| US3574181A (en) * | 1968-01-18 | 1971-04-06 | Sandoz Ltd | Disazo dyes |
| GB1394365A (en) * | 1972-01-28 | 1975-05-14 | Impperial Chemical Ind Ltd | Disperse azo dyestuffs |
| CH569762A5 (en) * | 1972-07-04 | 1975-11-28 | Sandoz Ag | Azo dyes contg thiophene ring - as disperse dyes for synthetic fibres with good resistance to light |
| CH554395A (en) * | 1972-07-11 | 1974-09-30 | Sandoz Ag | PROCESS FOR THE PRODUCTION OF PERSISTENTLY SOLUBLE AZO COMPOUNDS IN WATER. |
-
1973
- 1973-09-06 CH CH1281473A patent/CH584257A5/xx not_active IP Right Cessation
-
1974
- 1974-01-01 AR AR255508A patent/AR206123A1/en active
- 1974-08-30 DE DE2441524A patent/DE2441524A1/en active Pending
- 1974-09-02 NL NL7411613A patent/NL7411613A/en unknown
- 1974-09-03 US US05/502,445 patent/US4055556A/en not_active Expired - Lifetime
- 1974-09-03 GB GB3838674A patent/GB1471999A/en not_active Expired
- 1974-09-04 ES ES429754A patent/ES429754A1/en not_active Expired
- 1974-09-04 JP JP49100986A patent/JPS5051528A/ja active Pending
- 1974-09-04 AU AU72982/74A patent/AU7298274A/en not_active Expired
- 1974-09-05 BE BE148255A patent/BE819599A/en unknown
- 1974-09-06 BR BR7454/74A patent/BR7407454D0/en unknown
- 1974-09-06 IT IT52897/74A patent/IT1019202B/en active
- 1974-09-06 FR FR7430263A patent/FR2243194B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1471999A (en) | 1977-04-27 |
| IT1019202B (en) | 1977-11-10 |
| US4055556A (en) | 1977-10-25 |
| AU7298274A (en) | 1976-03-11 |
| AR206123A1 (en) | 1976-06-30 |
| FR2243194B1 (en) | 1978-04-28 |
| BR7407454D0 (en) | 1975-07-08 |
| BE819599A (en) | 1975-03-05 |
| JPS5051528A (en) | 1975-05-08 |
| NL7411613A (en) | 1975-03-10 |
| CH584257A5 (en) | 1977-01-31 |
| FR2243194A1 (en) | 1975-04-04 |
| DE2441524A1 (en) | 1975-03-13 |
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